Earmould impression kit - UK MHRA Medical Device Registration
Earmould impression kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 113057. The device is manufactured by Sonova UK Limited from England, United Kingdom, classified as General Medical Device.
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Device Type
General Medical Device
Devices
Earmould impression kit
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Feb 16, 2024
Address
Sonova House Lakeside Drive Centre Park Square
Warrington, England, United Kingdom
Created Date
May 5, 2021
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